Variant report

Variant	esv1793380
Chromosome Location	chr1:243044385-243184503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF1	chr1:243148543-243148578	K562	blood:	n/a	n/a
3	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
4	BATF	chr1:243174180-243174389	GM12878	blood:	n/a	n/a
5	BATF	chr1:243178561-243178941	GM12878	blood:	n/a	n/a
6	BATF	chr1:243178503-243178928	GM12878	blood:	n/a	n/a
7	BATF	chr1:243171378-243171664	GM12878	blood:	n/a	n/a
8	BATF	chr1:243182370-243182587	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:243178625-243178904	GM12878	blood:	n/a	chr1:243178799-243178808
10	BCL11A	chr1:243153505-243153675	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:243172627-243172798	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:243169760-243169972	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:243174177-243174356	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:243182297-243182573	GM12878	blood:	n/a	chr1:243182520-243182528 chr1:243182526-243182535
15	BCL11A	chr1:243178550-243178986	GM12878	blood:	n/a	chr1:243178799-243178808
16	BCL11A	chr1:243171382-243171573	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
18	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
19	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
20	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
21	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
22	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
23	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
24	CEBPB	chr1:243148513-243148717	K562	blood:	n/a	n/a
25	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
26	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
27	CEBPB	chr1:243118344-243118540	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
28	CEBPB	chr1:243118303-243118616	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
29	CEBPB	chr1:243118255-243118634	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
30	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
31	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
32	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
33	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
34	CEBPB	chr1:243118268-243118571	HepG2	liver:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
35	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
36	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
37	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
38	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
39	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
40	CTCF	chr1:243100156-243100355	GM10266	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
41	CTCF	chr1:243174120-243174270	AG04449	skin:	n/a	n/a
42	CTCF	chr1:243100080-243100230	HL-60	blood:	n/a	n/a
43	CTCF	chr1:243063909-243063983	ProgFib	skin:	n/a	n/a
44	CTCF	chr1:243045520-243045670	GM12865	blood:	n/a	n/a
45	CTCF	chr1:243174215-243174421	MCF-7	breast:	n/a	chr1:243174284-243174291
46	CTCF	chr1:243100073-243100432	GM12878	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
47	CTCF	chr1:243166373-243166535	LNCaP	prostate:	n/a	chr1:243166447-243166465 chr1:243166448-243166464
48	CTCF	chr1:243100021-243100450	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
49	CTCF	chr1:243100162-243100338	GM13977	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
50	CTCF	chr1:243100160-243100310	MCF-7	breast:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243139525-243139575	SK-N-SH	brain:	n/a
2	chr1:243139525-243139575	SK-N-SH	brain:	n/a
3	chr1:243053865-243053915	IMR90	lung:	fetal
4	chr1:243050875-243050925	AG04449	skin:	fetal
5	chr1:243053673-243053723	HCM	heart:	n/a
6	chr1:243054071-243054121	HUVEC	blood vessel:	n/a
7	chr1:243057080-243057130	Jurkat	blood:	n/a
8	chr1:243050875-243050925	NH-A	brain:	n/a
9	chr1:243050875-243050925	GM12892	blood:	n/a
10	chr1:243057080-243057130	AoSMC	blood vessel:	n/a
11	chr1:243050875-243050925	ovcar-3	ovarian:	n/a
12	chr1:243053673-243053723	Hela-S3	cervix:	n/a
13	chr1:243053934-243053984	MCF-7	breast:	n/a
14	chr1:243053865-243053915	HRPEpiC	eye:	n/a
15	chr1:243053934-243053984	GM06990	blood:	n/a
16	chr1:243054071-243054121	HepG2	liver:	n/a
17	chr1:243050875-243050925	HMEC	breast:	n/a
18	chr1:243053425-243053475	GM12891	blood:	n/a
19	chr1:243053934-243053984	Caco-2	colon:	n/a
20	chr1:243139525-243139575	HUVEC	blood vessel:	n/a
21	chr1:243053673-243053723	NHBE	bronchial:	n/a
22	chr1:243053425-243053475	PFSK-1	brain:	n/a
23	chr1:243057080-243057130	NHBE	bronchial:	n/a
24	chr1:243054071-243054121	NB4	blood:	n/a
25	chr1:243053425-243053475	SK-N-SH_RA	brain:	n/a
26	chr1:243139525-243139575	ovcar-3	ovarian:	n/a
27	chr1:243053425-243053475	LNCaP	prostate:	n/a
28	chr1:243054071-243054121	PrEC	prostate:	n/a
29	chr1:243138527-243138577	ProgFib	skin:	n/a
30	chr1:243053865-243053915	HCT-116	colon:	n/a
31	chr1:243050875-243050925	MCF10A-Er-Src	breast:	n/a
32	chr1:243053934-243053984	AG04449	skin:	fetal
33	chr1:243053865-243053915	SK-N-SH	brain:	n/a
34	chr1:243053425-243053475	A549	lung:	n/a
35	chr1:243050875-243050925	HCM	heart:	n/a
36	chr1:243050875-243050925	HIPEpiC	eye:	n/a
37	chr1:243139525-243139575	NHDF-neo	bronchial:	n/a
38	chr1:243053865-243053915	GM12892	blood:	n/a
39	chr1:243057080-243057130	ECC-1	luminal epithelium:	n/a
40	chr1:243057080-243057130	SK-N-SH	brain:	n/a
41	chr1:243138527-243138577	ovcar-3	ovarian:	n/a
42	chr1:243139525-243139575	LNCaP	prostate:	n/a
43	chr1:243053865-243053915	NH-A	brain:	n/a
44	chr1:243053865-243053915	H1-hESC	embryonic stem cell:	embryo
45	chr1:243053934-243053984	AoSMC	blood vessel:	n/a
46	chr1:243139525-243139575	AoSMC	blood vessel:	n/a
47	chr1:243139525-243139575	GM12891	blood:	n/a
48	chr1:243053673-243053723	AG04450	lung:	fetal
49	chr1:243139525-243139575	AG04449	skin:	fetal
50	chr1:243057080-243057130	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
2	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
3	chr1:243174257..243175773-chr22:20004723..20006804,2	K562	blood:
4	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-3	chr1:243170676-243170770	XLOC_001282
2	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
3	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
4	lnc-CEP170-3	chr1:243169147-243169576	XLOC_001282
5	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-
6	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
7	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
8	lnc-CEP170-3	chr1:243169714-243169980	XLOC_001282

Variant related genes	Relation type
ENSG00000234116	TF binding region
ENSG00000230199	TF binding region
ENSG00000270818	TF binding region
ENSG00000264972	TF binding region
ENSG00000234116	CpG island
ENSG00000230199	CpG island
ENSG00000270818	CpG island
ENSG00000264972	CpG island
LEFTY2	miRNA target sites
LEPREL4	miRNA target sites

Extended variants
information (count: 1781 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35330804	chr1:243044407-243044408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs35576227	chr1:243044423-243044424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558673472	chr1:243044444-243044445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545438509	chr1:243044516-243044517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563730078	chr1:243044533-243044534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576096825	chr1:243044560-243044561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144842842	chr1:243044608-243044609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563478024	chr1:243044618-243044619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562804398	chr1:243044620-243044621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573876222	chr1:243044760-243044761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542873197	chr1:243044786-243044787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372583723	chr1:243044789-243044790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138258809	chr1:243044823-243044824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114791184	chr1:243044853-243044854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189639198	chr1:243044867-243044868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551395984	chr1:243044889-243044890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77944505	chr1:243044951-243044952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35105770	chr1:243044962-243044963	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs550914097	chr1:243044966-243044967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35705897	chr1:243044998-243044999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567811661	chr1:243045000-243045001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs36084319	chr1:243045002-243045003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536550690	chr1:243045027-243045028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141838361	chr1:243045029-243045030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561942844	chr1:243045067-243045068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566821345	chr1:243045074-243045075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3003549	chr1:243045081-243045082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35261722	chr1:243045106-243045107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558511382	chr1:243045120-243045121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34863369	chr1:243045128-243045129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575360052	chr1:243045164-243045165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34176754	chr1:243045169-243045170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35923705	chr1:243045224-243045225	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs544429900	chr1:243045258-243045259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185876773	chr1:243045275-243045276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566555629	chr1:243045294-243045295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35083058	chr1:243045314-243045315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35864981	chr1:243045318-243045319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34567501	chr1:243045368-243045369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529047346	chr1:243045418-243045419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10926902	chr1:243045431-243045432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542563123	chr1:243045469-243045470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190684206	chr1:243045479-243045480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575110392	chr1:243045620-243045621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545058167	chr1:243045624-243045625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564844996	chr1:243045695-243045696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149368500	chr1:243045712-243045713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544253041	chr1:243045727-243045728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147510698	chr1:243045732-243045733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12029605	chr1:243045760-243045761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:243041000-243046600	Weak transcription	Pancreas	Pancrea
2	chr1:243042200-243044400	Weak transcription	Fetal Heart	heart
3	chr1:243044400-243045400	Enhancers	Fetal Heart	heart
4	chr1:243046600-243046800	Enhancers	Pancreas	Pancrea
5	chr1:243046800-243053600	Weak transcription	Pancreas	Pancrea
6	chr1:243047200-243049000	Weak transcription	A549	lung
7	chr1:243049000-243049200	Enhancers	A549	lung
8	chr1:243049200-243049800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:243049200-243049800	Enhancers	Liver	Liver
10	chr1:243049200-243049800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr1:243049200-243049800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr1:243049200-243049800	Flanking Active TSS	A549	lung
13	chr1:243049200-243049800	Enhancers	HepG2	liver
14	chr1:243049600-243049800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:243049800-243050600	Enhancers	A549	lung
16	chr1:243049800-243053600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:243049800-243053600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:243050600-243051800	Weak transcription	A549	lung
19	chr1:243053400-243053600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:243053600-243053800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr1:243053600-243054000	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr1:243053600-243054000	Active TSS	H1 Cell Line	embryonic stem cell
23	chr1:243053600-243054000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:243053600-243054000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:243053600-243054000	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:243053600-243054000	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr1:243053600-243054000	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr1:243053600-243054000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:243053600-243054000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:243053600-243054000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
33	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:243053600-243054000	Bivalent Enhancer	Brain Hippocampus Middle	brain
36	chr1:243053600-243054000	Enhancers	Fetal Brain Male	brain
37	chr1:243053600-243054000	Bivalent/Poised TSS	Fetal Brain Female	brain
38	chr1:243053600-243054000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr1:243053600-243054000	Enhancers	Pancreas	Pancrea
40	chr1:243053600-243054000	Enhancers	Placenta Amnion	Placenta Amnion
41	chr1:243053600-243054000	Bivalent Enhancer	HMEC	breast
42	chr1:243053600-243054200	Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr1:243053600-243054200	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr1:243053600-243054200	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr1:243053600-243054200	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr1:243053600-243054200	Active TSS	Brain Germinal Matrix	brain
47	chr1:243053600-243054200	Active TSS	HSMM	muscle
48	chr1:243053800-243054000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr1:243053800-243054000	Bivalent Enhancer	Colonic Mucosa	Colon
50	chr1:243053800-243054200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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